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CAS 160842-62-6

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3-(TERT-BUTYL)-1-METHYL-1H-PYRAZOLE-5-CARBONYL CHLORIDE

Description:
3-(Tert-butyl)-1-methyl-1H-pyrazole-5-carbonyl chloride is a chemical compound characterized by its pyrazole ring structure, which is a five-membered aromatic ring containing two nitrogen atoms. The presence of a tert-butyl group enhances its hydrophobic properties, while the carbonyl chloride functional group (acyl chloride) makes it reactive, particularly towards nucleophiles. This compound is typically used in organic synthesis, particularly in the preparation of various derivatives and intermediates in pharmaceutical chemistry. Its reactivity allows it to participate in acylation reactions, making it valuable in the development of bioactive molecules. The compound is likely to be a solid at room temperature and may have specific solubility characteristics depending on the solvent used. Safety precautions should be taken when handling this compound, as carbonyl chlorides can be corrosive and may release harmful gases upon reaction with water or alcohols. Overall, its unique structural features and reactivity profile make it an important compound in synthetic organic chemistry.
Formula:C9H13ClN2O
InChI:InChI=1/C9H13ClN2O/c1-9(2,3)7-5-6(8(10)13)12(4)11-7/h5H,1-4H3
SMILES:CC(C)(C)c1cc(C(=O)Cl)n(C)n1
Synonyms:
  • Buttpark 43\57-64
  • 3-(Tert-Butyl)-1-Methylpyrazole-5-Carbonyl Chloride
  • Timtec-Bb Sbb005464
  • 1H-Pyrazole-5-carbonyl chloride, 3-(1,1-dimethylethyl)-1-methyl- (9CI)
  • 3-(tert-Butyl)-1-methylpyrazole-5-carbonyl
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